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Liver lesions
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== '''Non-cirrhotic liver''' == * '''Cavernous haemangioma''' ** Commonest hepatic lesion *** Generally 30-50yo, F:M 3:1 *** Normal AFP ** Benign - blood-filled spaces with slowly-moving blood *** Subtype: giant haemangioma, which can show up with a central scar *** Sclerosed - occurs after infarction. Capsular retraction, scarring. *** Haemangiomatosis - rare - diffuse replacement of liver by haemangiomas ** Features *** USS **** Hyperechoic, with no hypoechoic rim **** No flow on doppler **** USS contrast agents can be used to clinch the diagnosis *** CT **** Noncon: well-demarcated hypodense mass **** Arterial: discontinuous, nodular peripheral enhancement **** PV: progressive peripheral enhancement with more centripetal fill-in **** Delayed: further irregular fill-in, therefore iso or hyper attenuating to liver parenchyma **** Rim enhancement is NEVER a haemangioma **** *** Edge often lobulated *** Progressive infilling *** MRI is the best test **** Very high t2 signal **** Follows blood pool in terms of contrast signal * '''Focal nodular hyperplasia''' ** Common, especially in young female adults (9:1 F:M, age 35-50) ** Very rarely symptomatic ** Hypoplastic result to vascular insult ** Characteristic fibrous scar in centre of lesion ** Findings *** Central scar - 40-60% - high T2 signal **** Beware the central scar!!! Not diagnostic of FNH *** USS - often subtle *** CT - **** Noncon: hypo or isodense lesion with hypoattenuating centre **** Arterial: avid uniform arterial enhancement, except for hypoattenuating central scar **** PV: no washout (it FADES rather than WASHES OUT - that is, still brighter than normal liver on PV), microlobulated border. Usually slightly brighter than background normal liver in PV phase. **** Delayed: mostly get enhancement of fibrotic scar *** *** Invisible on pre-contrast, avid uniform arterial enhancement, slightly bright on PV, disappeared on late venous. * '''Hepatocellular adenoma''' ** True monoclonal neoplasms *** Can progress to HCC ** Less common than FNH ** Age 20-40 ** Usually women (F:M 9:1) ** 80% are single lesions ** A/w: *** Rupture *** Growth in response to oestrogen/testosterone *** Malignant transformation to HCC *** Glycogen storage diseases *** Metabolic syndrome ** CT *** Often look identical to FNH *** Liver-specific contrast is necessary - these are usually dark in primovist phases *** Noncon: well-demarcated, hypo or isodense lesion *** Arterial: peripheral enhancement *** PV: centripetal flow *** Delayed: iso or hypodense *** * '''Liver mets''' ** CT/MRI *** '''Rim enhancement''' on arterial phase, with early washout *** PV: progressive enhancement of a thickened rind *** Delayed: usually hypoattenuating (washout), but occasionally have delayed enhancement due to desmoplastic reaction *** Dark on primovist phases (don't contain hepatocytes to take up the contrast) *** Central necrosis common *** ** Hypervascular mets *** Neuroendocrine most common *** RCC *** Melanoma *** Thyroid *** Choriocarcinoma ** Screening for liver mets - primovist MRI is best * '''Intrahepatic cholangiocarcinoma''' ** RFs: *** Cirrhosis *** HBV *** HCV ** CT *** Noncon: homogenous hypoattenuating mass *** Arterial: Rim type arterial phase hyperenhancement around a hypodense lesion *** PV: progressive enhancement with centripetal filling *** Delayed: iso or hypodense due to abundant fibrosis stroma *** Capsular reaction *** Satellite nodules *** Delayed, cloud-like infilling of central stroma *** * Hepatic angiomyolipoma ** Seen in a/w tuberous sclerosis, or sporadically * Fibrolamellar HCC ** Very rare, usually adolescents or young adults, without cirrhosis ** Large well-defined mass with large scar ** Arterial enhancement with washout ** Calcification common ** * Epithelioid haemangioendothelioma ** Multi-focal lesions ** Geographical ** Capsular retration * Hydatid cyst ** ** Parasitic infection with tapeworm ** Hypodense lesion with hyperattenuating wall ** Detachment of laminated membrane from pericyst can be visualised as linear areas of hyperattenuation ** Daughter cysts are located peripherally within the mother cyst; they are usually at a lower density than the mother cyst * Polycystic liver disease ** * Biliary cystadenoma and cystadenocarcinoma ** * Simple hepatic cysts ** Homogenous hypoattenuation (0-10HU) ** Imperceptible wall ** No internal structures ** No enhancement after IV contrast **
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